long QT syndrome 11

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Summary

Literature (0)

DOID:0110652 - long QT syndrome 11

Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2.

Synonyms: LQT11

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: akap9

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012738 - long QT syndrome 11

MONDO:0012738 - long QT syndrome 11

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), long QT syndrome (is_a)